25GA Illuminating Laser Probe - Alcon

GUDID 10632307000741

25GA Illuminating Laser Probe - Alcon

PEREGRINE SURGICAL, LTD.

Ophthalmic laser system beam guide

• Primary Device ID: 10632307000741
• NIH Device Record Key: e8d35e1a-bf42-41a4-8e2e-2a05141a008f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: 25GA Illuminating Laser Probe - Alcon
• Version Model Number: PD725.30
• Company DUNS: 622467348
• Company Name: PEREGRINE SURGICAL, LTD.
• Device Count: 1
• DM Exempt: true
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(215)348-0456
• Email: jayne@peregrine-surgical.com
• Phone: +1(215)348-0456
• Email: jayne@peregrine-surgical.com
• Phone: +1(215)348-0456
• Email: jayne@peregrine-surgical.com
• Phone: +1(215)348-0456
• Email: jayne@peregrine-surgical.com
• Phone: +1(215)348-0456
• Email: jayne@peregrine-surgical.com
• Phone: +1(215)348-0456
• Email: jayne@peregrine-surgical.com
• Phone: +1(215)348-0456
• Email: jayne@peregrine-surgical.com
• Phone: +1(215)348-0456
• Email: jayne@peregrine-surgical.com
• Phone: +1(215)348-0456
• Email: jayne@peregrine-surgical.com
• Phone: +1(215)348-0456
• Email: jayne@peregrine-surgical.com
• Phone: +1(215)348-0456
• Email: jayne@peregrine-surgical.com
• Phone: +1(215)348-0456
• Email: jayne@peregrine-surgical.com
• Phone: +1(215)348-0456
• Email: jayne@peregrine-surgical.com
• Phone: +1(215)348-0456
• Email: jayne@peregrine-surgical.com
• Phone: +1(215)348-0456
• Email: jayne@peregrine-surgical.com

Device Dimensions

• Needle Gauge: 25 Gauge
• Needle Gauge: 25 Gauge
• Needle Gauge: 25 Gauge
• Needle Gauge: 25 Gauge
• Device Size Text, specify: 0
• Needle Gauge: 25 Gauge
• Device Size Text, specify: 0
• Needle Gauge: 25 Gauge
• Device Size Text, specify: 0
• Needle Gauge: 25 Gauge
• Device Size Text, specify: 0
• Needle Gauge: 25 Gauge
• Device Size Text, specify: 0
• Needle Gauge: 25 Gauge
• Device Size Text, specify: 0
• Needle Gauge: 25 Gauge
• Device Size Text, specify: 0
• Needle Gauge: 25 Gauge
• Device Size Text, specify: 0
• Needle Gauge: 25 Gauge
• Device Size Text, specify: 0
• Needle Gauge: 25 Gauge
• Device Size Text, specify: 0
• Needle Gauge: 25 Gauge
• Device Size Text, specify: 0
• Needle Gauge: 25 Gauge
• Device Size Text, specify: 0
• Needle Gauge: 25 Gauge
• Device Size Text, specify: 0
• Needle Gauge: 25 Gauge

Device Identifiers

Device Issuing Agency	Device ID
GS1	00632307000744 [Primary]
GS1	10632307000741 [Package]; Contains: 00632307000744; Package: Box [5 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K031023

FDA Product Code

• HQF: Laser, ophthalmic

Sterilization

• Steralize Prior To Use: true
• Device Is Sterile: true

[10632307000741]

Ethylene Oxide

[10632307000741]

Ethylene Oxide

[10632307000741]

Ethylene Oxide

[10632307000741]

Ethylene Oxide

[10632307000741]

Ethylene Oxide

[10632307000741]

Ethylene Oxide

[10632307000741]

Ethylene Oxide

[10632307000741]

Ethylene Oxide

[10632307000741]

Ethylene Oxide

[10632307000741]

Ethylene Oxide

[10632307000741]

Ethylene Oxide

[10632307000741]

Ethylene Oxide

[10632307000741]

Ethylene Oxide

[10632307000741]

Ethylene Oxide

[10632307000741]

Ethylene Oxide

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2016-05-06

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